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U.S. Department of Health and Human Services

Manufacturer and User Facility Device Experience (MAUDE)

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Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
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78 records meeting your search criteria returned- Product Code: DQO Product Problem: Occlusion Within Device Report Date From: 01/1/2007

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ManufacturerBrand NameDate Report Received
CORDIS CASHEL UNKNOWN TRAPEASE PERMANENT VENA CAVA FIL 10/05/2017
Unknown Manufacturer UNKNOWN TRAPEASE PERMANENT VENA CAVA FIL 09/28/2017
CORDIS CASHEL 466P306X 09/28/2017
CORDIS CASHEL UNKNOWN TRAPEASE PERMANENT VENA CAVA FIL 09/22/2017
CORDIS CASHEL TRAPEASE PVCF FEM/JUG 55CM CSI 09/03/2017
CORDIS CASHEL UNKNOWN VENA CAVA FILTER 08/11/2017
CORDIS CASHEL TRAPEASE PVCF FEM/JUG 55CM CSI 07/17/2017
CORDIS CASHEL TRAPEASE PVCF FEM/JUG 55CM CSI 07/05/2017
CORDIS CASHEL TRAPEASE PVCF FEM/JUG 55CM CSI 07/03/2017
CORDIS CASHEL TRAPEASE PVCF FEM/JUG 55CM CSI 06/26/2017
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